Lead Biostatistician, Clinical Trials Analytics

ICON Strategic Solutions; Paris; Sur place; EUR 65 000 - 95 000; Plein temps

Avantages offerts par ce poste

Health insurance

Competitive retirement planning

Life assurance

Global Employee Assistance Programme

Résumé du poste

ICON plc is a world-leading healthcare intelligence and clinical research organization. The Senior Biostatistician I will design and analyse clinical trials, interpreting complex medical data to advance innovative treatments and therapies.

This role is based in Paris, France, and involves leading biostatistics tasks with a strong focus on quality and continuous improvement. The candidate will develop analysis plans, contribute to CRF design, perform analyses, and collaborate with

Qualifications

• Master's degree or Ph.D in Biostatistics or related field with 5+ years biostatistical experience.
• Strong knowledge of multiple statistical and therapeutic areas and drug development processes.
• Excellent problem-solving and attention to detail.
• Effective communication to collaborate with multidisciplinary teams.

Responsabilités

• Lead biostatistics tasks with technical depth and quality focus.
• Develop statistical analysis plans and reporting specifications.
• Manage statistical aspects of CRF design and edit specifications.
• Perform statistical analyses and interpret results across studies.
• Review randomization specifications and dummy schemes.
• Participate in bid defense meetings.

Connaissances

Biostatistics expertise

Clinical trial analysis

Statistical programming

Independent work

Communication skills

Formation

Master's degree or PhD in Biostatistics

Outils

SAS

R

Description du poste

ICON plc is a world-leading healthcare intelligence and clinical research organization. The Senior Biostatistician I will design and analyse clinical trials, interpreting complex medical data to advance innovative treatments and therapies.

This role is based in Paris, France, and involves leading biostatistics tasks with a strong focus on quality and continuous improvement. The candidate will develop analysis plans, contribute to CRF design, perform analyses, and collaborate with